|Publication number||US4839155 A|
|Application number||US 07/094,507|
|Publication date||Jun 13, 1989|
|Filing date||Sep 9, 1987|
|Priority date||Sep 11, 1986|
|Also published as||DE3762617D1, EP0260066A1, EP0260066B1|
|Publication number||07094507, 094507, US 4839155 A, US 4839155A, US-A-4839155, US4839155 A, US4839155A|
|Original Assignee||National Research Development Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (1), Non-Patent Citations (24), Referenced by (59), Classifications (28), Legal Events (7)|
|External Links: USPTO, USPTO Assignment, Espacenet|
1. Field of the invention
This invention relates to derivatives of tamoxifen, their preparation and use in therapy and diagnosis of breast cancer.
2. Description of prior art
Tamoxifen is Z (1,2-diphenyl)-1-[4-(2-dimethylaminoethoxy)-phenyl]-1-butene of formula (1) ##STR2##
Its anti-estrogenic properties have led since 1971 to its clinical use in the treatment of malignant tumors, especially estrogen receptor-positive (hormone-dependent) breast cancer.
Tamoxifen has a relatively low affinity for the estrogen receptor (ER). Attempts have therefore been made to find tamoxifen derivatives having improved ER affinity. Changes have been made in virtually every part of the molecule. One derivative which at first seemed promising was the 4-hydroxy derivative of formulat (2) ##STR3## in which X=--OH. This compound was shown by in vitro tests to be a potent anti-estrogen, but unfortunately proved in vivo to be less effective than tamoxifen, owing to rapid glucuronidation of the hydroxyl group followed by excretion.
Several derivatives of tamoxifen are known which have other 4-position substituents, in which X is methoxy, methyl, fluoro or chloro. These compounds have been evaluated by K. E. Allen et al., British Journal of Pharmacology 71, 83-91 (1980). The methyl, chloro and fluoro derivatives were of particular interest as they are unlikely to be metabolised to the 4-hydroxy derivative and thence glucuronidated. An in vitro test of estrogen receptor affinity indicated that tamoxifen was approximately equiactive with its 4-methyl, fluoro- and chloro-derivatives. In vivo rat uterine weight tests indicated that these derivatives has lower anti-estrogenic activity than tamoxifen. Other tests indicated that the activity of the 4-methoxy derivative was about the same as tamoxifen.
It has now been found that the 4-iodo derivative (formula 2: X=iodo) has greater potency than tamoxifen in relation to estrogen receptor-positive breast cancer. In view of the report by K. E. Allen et al., supra, that the 4-fluoro and 4-chloro compounds are (at best) of no greater potency than tamoxifen, the present finding is most surprising. Also, the 4-bromo, 3-iodo and 3-bromo analogues show promise as alternatives to tamoxifen of at least equal potency.
These tamoxifen derivatives, which are named E 1-[4-(2-dimethylaminoethoxy)phenyl]-1-(3- and 4-iodophenyl)-2-phenyl-1-butene and E 1-[4-(2-dimethylaminoethoxy)phenyl]-1-(3- and 4-bromophenyl)-2-phenyl-1-butene, are believed to be new compounds. Analogues thereof in which the dimethylamino group is replaced by other dialkylamino groups or by monoalkylamino groups or a nitrogen-containing saturated heterocyclic ring are also believed to be novel and are potent against ER-positive breast cancer. Accordingly, the present invention provides 3- and 4-iodo and -bromotamoxifen derivatives which are compounds of formula (3) ##STR4## wherein X represents 3- or 4- iodo or bromo and the R1 and R2 symbols, which may be the same or different, represent C1-3 alkyl, especially methyl or ethyl, groups or R1 represents a hydrogen atom and R2 a C1-3 alkyl group or R1 and R2 together with the nitrogen atom to which they are attached represent a saturated heterocyclic group, typically having 5 or 6 ring atoms, especially a pyrrolidino, piperidino, 4-methylpiperidino or morpholino group, and their pharmaceutically acceptable acid addition salts.
The invention further includes:
the 3- and 4-iodo and -bromotamotamoxifen derivatives, i.e. the compounds of formula (3) and their pharmaceutically acceptable addition salts for use in treatment of ER-positive breast cancer;
the 3- and 4-iodo and -bromotamoxifen derivatives for use in the preparation of a medicament for treatment of ER-positive breast cancer or, where national patent law permits, a method of treating such a cancer in a human patient which comprises administering to the patient a therapeutically effective amount of the tamoxifen derivative;
a pharmaceutical composition comprising a 3- or 4-iodo or -bromotamoxifen derivative in association with a pharmaceutically effective diluent, carrier or excipient;
a process for the preparation of the 3- and 4-iodo and -bromotamoxifen derivatives which comprises reacting 1-[4-(2-chloroethoxy)phenyl]-2-phenyl-1-butene with an organometallic reagent derived from 1,3- or 1,4-diiodo- or -dibromobenzene and capable of addition to a ketone group, in a substantially anhydrous organic solvent, to form a tertiary alcohol, dehydrating the tertiary alcohol to eliminate a molecule of water and thereby form 1-[4-(2- chloroethoxy)-phenyl]-1-(3- or 4-iodophenyl or -bromophenyl)-2-phenyl-1-butene as an isomeric mixture, separating the E isomer and reacting the E isomer with an amine of formula NR1 R2, R1 and R2 being defined as above; and
a process for the preparation of the 3- and 4-iodo and -bromo tamoxifen derivatives which comprises reacting a ketone of formula (4) ##STR5## R1 and R2 beind defined as above, in one step with an organometallic reagent as defined above, in a substantially anhydous orgaic solvent, to form a tertiary alcohol, dehydrating the tertiary alcohol to eliminate a molecule of water and thereby form 1-[4-(2-NR1 R2 -substituted ethoxy)phenyl]-1-(3- or 4-iodophenyl or 4-bromophenyl)-2-phenyl-1-butene as an isomeric mixture, and separating the E isomer.
The iodotamoxifen derivatives of the invention include per se those wherein the iodine atoms comprise radioisotopic iodine atoms. Predominantly useful such atoms are 125 I for radiotherapy of estrogen receptor-positive breast cancers and 131 I and 123 I which are gamma-emitters and therefore useful in imaging the tumours. These compounds, for such uses as well as per se, are part of the invention.
The radioisotopic iodotamoxifen derivatives can be prepared by a process comprising reacting a compound of formula ##STR6## wherein R1 and R2 are as defined in connction with formula (3) and Y represents a 3- or 4-substituent, whether an atom or a group, capable of being cleaved from its benzene ring (including within this definition a non-radioisotopic iodine atom), with a reagent capable of effecting such cleavage and with a source of radioisotopic iodine (which can be added as molecular iodine or iodide ions according to the cleavage-effecting reagent used and other reaction conditions). Preferably Y is chloro, bromo, iodo or amino.
The iodo derivatives are preferred to the bromo, and the 4-iodo to the 3-iodo. Preferably R1 and R2 are both alkyl groups, most preferably methyl, or NR1 R2 is pyrrolidino.
The compounds of formula (3) and their salts are prepared starting from ketones which are known compounds. The preferred reagent for the preparation of the organometallic halobenzene species is n-butyllithium. Alternatively the magnesium Grignard reagent can be used. The immediate product of the organometallic reaction is a tertiary alcohol which is then dehydrated to eliminate a molecule of water and thereby provide the ethylenic double bond required. The dehydration is preferably carried out by heating the alcohol in a strong acid such as concentrated hydrochloric acid. A mixture of isomers is produced of which the desired one is that in which the ethyl group and the (2-aminoethoxy)phenyl group are trans. The Z/E nomenclature designates this as Z for tamoxifen itself and E for the iodo or bromo derivatives.
In one embodiment of the invention, the starting ketone already contains the (2-aminoethoxy)phenyl group and therefore the reaction can be carried out in one step (since the tertiary alcohol need not be isolated). The isomer separation is then carried out on the end product.
Alternatively, the starting ketone contains the (2-chloroethoxy)phenyl group. The dehydration to the olefin yields the (2-chloroethoxy)phenyl intermediate. The isomers can be separated by crystallisation, which is very convenient, and the desired E isomer appropriately aminated by reaction with the alkylamine or heterocyclic amine required. The amination can be carried out in any manner known in the synthesis of tamoxifen, for example heating the chloroethoxy intermediate with the amine in a sealed vessel.
The acid addition salts can be prepared in any manner analogous to those of taoxifen, at any appropriate stage of the overall synthesis after formation of the tertiary alcohol. Usually they will be prepared as the final stage. Examples of such salts are the hydrochloride, sulphate, phosphate, acetate and citrate. In the "direct" method of preparation of the iodo or bromotamoxifen derivatives, an acid addition salt is formed under the acidic dehydration conditions used. This will ordinarily be neutralised with, say, sodium hydroxide. The isomers can then be separated either as the free bases or, after adding a approximately stoichiometric proportion of acid, as acid addition salts.
For pharmaceutical formulation, the iodo and bromotamoxifen derivatives can be formulated in the same or a similar way to tamoxifen and administered similarly and in about the same dose. Preferably they are formulated as tablets.
The iodotamoxifen derivatives include those wherein the iodine atoms in some or all of the molecules of a given sample have a radioisotopic (a radioactive or "hot") iodine atom. Predominantly useful such atoms are 125 I which emits low energy electrons having a short, sub-cellular range and 131 I and 123 I which emit gamma rays. The 125 I isotopic iodine is useful in the therapy of tumour cels containing oestrogen receptors, in the same manner as has already been reported for another 125 I tamoxifen derivative in which the iodine atom is attached to the same benzene ring as the 2-dimethylaminoethoxy group, in the ortho position thereto, see W. D. Bloomer et al., Int. J. Radiat. Biol, 38, 197-202 (1980). The 123 I and 131 I isotopes, of which 131 I is preferred, are gamma emitters and therefore usable for imaging of oestrogen receptor-carrying tumour cells. The use of all these three isotopes in another iodotamoxifen, namely that in which the iodine atom is present in the "diagonally opposite" position to that of formula (3), that is to say is para in the benzene ring attached to the carbon atom to which the ethyl group is also attached, is suggested by D. H. Hunter et al., Can. J. Chem. 61, 421-426 (1983). The content of radioisotopic iodine in the iodotamoxifen formulation should be adjusted to conform to conventional radiotherapy and imaging practice.
The commonly used radioisotopes of iodine have a short half-life, for 131 I 8 days, for 125 I 60 days, and for 123 I 13 hours. It is therefore necessary to prepare the radioisotopic compounds of the invention only shortly before the expected time of use. One suitable method of preparation, referred to above, starts from the corresponding compound substituted by non-radioactive ("cold") X (X=bromo or iodo) or by some other atom or group, for example chloro or amino, capable of undergoing a reaction in which the cold X or other atom or group is pulled off or cleaved from the benzene ring of the tamoxifen molecule.
In one aspect the starting compound is the "cold" iodotamoxifen, which is reacted with a copper (I) or (II) salt and an appropriate source of "hot" (radioisotopic) iodide such as sodium iodide. This a modified version of the Rosenmund-von Braun reaction in which an aryl iodide is convertible to the aryl cyanide by the action of copper (I) cyanide. Since this method does not give an iodotamoxifen product having a high proportion of its iodine atoms in radioisotopic form, it is not well suited to the production of iodotamoxifen for imaging purposes.
Another embodiment comprises reacting the starting compound containing the "cold" X with an alkyllithium and "hot" molecular iodine, in an inert atmosphere. The reaction mechanism is illustrated below using bromine as the cleavable atom and t-butyl lithium as the reagent which effects the cleavage. Ar denotes the residue of the tamoxifen molecule. ##STR7## Other alkyllithium reagents could be used in place of t-butyl lithium. The reaction takes place in a non-oxidising atmosphere in order to avoid production of a hydroxytamoxifen and a reducing atmosphere such as would react with molecular iodine is also to be avoided. An inert atmosphere is therefore the most suitable.
The reaction temperature can be any appropriate to the reaction equilibrium but is usually in the range of -80° to +20° C. A solvent is normally required and can be any appropriate to the temperature. Tetrahydrofuran is preferred at low temperatures. The iodine should be added in stoichiometric excess for the reaction. Preferably the radioisotopic iodine is added portionwise, less than the stoichiometric amount being added initially, whereby up to half of the radioisotopic I2 molecules added will become incorporated in the tamoxifen molecule. Addition of the remainder of the iodine, to a stoichiometric excess in total, as "cold" iodine will ensure that there is no avoidable wastage of the radioisotope. Of course, some of it (theoretically a half) will be wasted as iodide ions, which, however, can be recovered by methods known to those skilled in the raadioisotope art.
It will be seen that the 4-bromotamoxifen derivatives of formula (3) are useful as intermediates in the preparation of radioisotopic 4-iodotamoxifen derivatives. When a 4-chlorotamoxifen is used as the starting compound, it can be prepared analogously to the 4-bromotamoxifen derivatives described herein. The amino group of the 4-amino analogue can be cleaved and iodine substituted by the action of hyponitrous acid and radiolabelled sodium iodide.
Another method proceeds via a tributyltin intermediate, which can be stored and then converted to the iodotamoxifen immediately before use. This intermediate can be prepared by reacting the 4-bromo- or iodotamoxifen derivative with n-butyllithium (as described above) and then with tributyl tin chloride. This method has been described by W. D. Bloomer et al., supra.
Other methods of introducing a radioactive iodine atom will be found in R. H. Seevers and R. E. Counsel, Chem. Rev. 82, 575-590 (1982) and such methods are usable mutatis mutandis in the context of the present invention.
The following Examples illustrate the invention. Examples 1-6 illustrate preparation of iodo and bromotamoxifen derivatives. "Ether" means diethyl ether. Examples 7 and 8 indicate antiestrogenic effects of the derivatives and Example 9 a pharmaceutical composition. Examples 10 and 11 illustrate preparation of radioisotopic iodotamoxifen derivatives.
A stirred solution of 1,4-diiodobenzene (4.21 g, 12.7 mmol) in dry tetrahydrofuran (20 ml) was cooled under nitrogen by a dry ice-acetone bath. n-Butyllithium (8.5 ml of a 1.55M solution in hexane, 12.7 mmol) was added. After 5 minutes, a solution of 1-[4-(2-dimethylaminoethoxy)phenyl]-2-phenyl-1-butanone (2.0 g, 6.4 mmol) was added and the mixture allowed to warm to room temperature. After 15 hours, the mixture was poured into water (60 ml) and extracted with ether (2×50 ml). The ether extracts were concentrated and the residual oil dissolved in ethanol (20 ml). Concentrated hydrochloric acid (10 ml) was added and the mixture heated under reflux for 4 hours, then cooled, and poured into water (100 ml). The solution was basified with aqueous sodium hydroxide (3M) and extracted with ether (100 ml). The ether extract was dried with sodium sulphate, concentrated, and the residue applied to a column of silica (Merck 15111, 80 g). Elution with 1:1 light petroleum (b.p. 40°-60° C.-ether containing an increasing proportion of triethylamine gave after a forerun of tamoxifen which was discarded, at 5% triethylamine, a mixture of 4-iodotamoxifen and its Z isomer:-
______________________________________(i) 241 mg consisting of 3:1 trans (E):cis (Z) isomers(ii) 363 mg consisting of 1:1 trans (E):cis as determined (Z) isomers by NMR(iii) 406.5 mg consisting of 1:2 trans (E):cis (Z) isomers______________________________________
The total yield of products was 1.01 g (32%).
Recrystallisation of band (i) above gave a sample of the title compound, pure trans (E) isomer, m.p. 112°-114° C. (from light petroleum, b.p. 40°-60° C.). Found C, 62.88; H, 5.72; N, 2.79; I, 25.30%. C26 H28 INO requires C, 62.78; H, 5.67; N, 2.82; I, 25.51% NMR: δH (CDCl3, 250 MHz) 0.91 (3H, t J 7.4 Hz, CH3 CH2), 2.28 (6 H, s, NMe2), 2.43 (2H, q, J 7.4 Hz, CH3 CH2), 2.64 (2H, t, J 5.8 Hz, OCH2 CH2 N), 3.92 (2H, t, J 5.8 Hz, OCH2 CH2 N), 6.55 (2H, d, J 8.8 Hz, H-3,5 of C-C6 H4 -0), 6.73 (2H, d, J 8.8 Hz, H- 2,6 of C-C6 H4 -0), 6.98 (2H, d, J 8.3 Hz, H-2,6 of C-C6 H4 -I), 7.04-7.22 (5H, m, Ph), 7.66 (2H, d, J 8.3 Hz, H-3,5 of C-C6 H4 -I); mass spectrum m/z 497 (M+, 36%), 380(3), 72(100), 58(100).
The cis (Z) isomer gave δH (CDCl3, 60 MHz) inter alia 2.32 (6H, s, NMe2), 4.07 (2H, t, J 6 Hz, OCH2 CH2 N).
A stirred solution of 1,4-dibromobenzene (6.88 g, 29.15 mmol) in dry tetrahydrofuran (30 ml) was cooled under nitrogen by a dry ice-acetone bath and n-butyllithium (15.1 ml of a 1.55M solution in hexane; 24 mmol) added over 2 minutes. A precipitate formed. After 10 minutes, a solution of 1-[4-(2-dimethylaminoethoxy)phenyl]-2-phenyl-1-butanone (6.09 g, 19.43 mmol) in tetrahydrofuran (15 ml) was added and the mixture allowed to warm to room temperature.
After 16 hours, the mixture was worked up as described above for 4-iodotamoxifen to give crude tertiary alcohol as a solid, which was dissolved in ethanol (100 ml). Concentrated hydrochloric acid (60 ml) was added and the mixture heated up under reflux for 20 hours. Work up was as described above for 4-iodotamoxifen. The crude product was dissolved in hot light petroleum (b.p. 80°-100° C.) (40 ml). Cooling gave crystals of the title compound, i.e. the trans (E) isomer, (2.78 g, 32% yield). The mother liquors were applied to a column of silica (60 g). Elution with 20:20:1 light petroleum (b.p. 40°-60° C.)-ether-triethylamine gave
(i) 4.36 g oil consisting of 2.5:1 Z:E isomers
(ii) 0.58 g oil consisting of 4:1 Z:E isomers
The total yield was 7.72 g, 88%. The proportion of isomers in the crude product was estimated as 1.2:1.
Recrystallisation of (i) gave further trans (E) isomer, 0.19 g, then cis (Z) isomer, 1.10 g.
In a repeat of this reaction, but using a milder dehydration procedure (25 ml conc. HCl, 200 ml ethanol, reflux 30 minutes) the ratio of isomers in the crude product was improved to 1.6:1 but the yield was lower, 72% (35% yield of trans (E) isomer isolated following crystallisation).
The trans (E) isomer, 4-bromotamoxifen, had m.p. 114°-116° C. (from light petroleum, b.p. 80°-100° C.). Found C, 69.44; H, 6.29; N, 2.92; Br, 17.88. C26 H28 BrNO requires C, 69.32; H, 6.26; N, 3.11; Br, 17.74%; NMR: δH (CDCl3, 250 MHz) 0.91 (3H, t, J 7.4 Hz, CH3 CH2), 2.28 (6H, s, NMe2), 2.44 (2H, q, J 7.4 Hz, CH3 CH2), 2.64 (2H, t, J 5.7 Hz, OCH2 CH2 N), 3.92 (2H, t, J 5.7 Hz, OCH2 CH2 N), 6.56 (2H, d J 8.8 Hz, ArH ortho to OR), 6.73 (2H, d, J 8.8 Hz, ArH meta to OR), 7.08-7.26 (7H, m, ArH), 7.46 (2H, d, J 8.3 Hz, ArH ortho to Br).
The cis (Z) isomer had m.p. 77°-78° C. (from light petroleum, b.p. 80°-100° C.). Found C, 69.49; H, 6.31; N, 3.05; Br, 17.70. C26 H28 BrNO requires C, 69.33; H, 6.27; N, 3.11; Br, 17.74%; δH (CDCl3, 60 MHz), 0.90 (3H, t, J 7 Hz, CH3 CH2), 2.31 (6H, s, NMe2), 2.48 (2H, q, J 7 Hz, CH3 CH2), 2.71 (2H, t, J 6 Hz, OCH2 CH2 NMe2), 4.06 (2H, t, J 6 Hz, OCH2 CH2 NMe2), 6.62 (2H, d, J 9 Hz, ArH ortho to OR), 6.9-7.3 (11H, m, ArH).
1-[4-(2-chloroethoxy)phenyl]-2-phenyl-1-butanone has been prepared by R. McCague, J. Chem. Research, 1986, (S), 58-9; (M), 771-93, by Friedel-Crafts condensation of 2-phenylbutanoic acid and (2-chloroethoxy)benzene. 2-Phenylbutanoic acid is commercially available. (2-Chloroethoxy)benzene is obtainable by alkylation of phenol with 1,2-dichloroethane or by reaction of 2-phenoxyethanol with thionyl chloride.
A stirred solution of 1,4l -diiodobenzene (21.8 g, 66 mmol) in dry tetrahydrofuran (100 ml) under nitrogen was cooled to ca.-75° C. and n-butyllithium (41.2 ml of a 1.6M solution in hexane, 66 mmol) introduced over 5 minutes. After 10 minutes, a solution of 1-[4-(2-chloroethoxy)phenyl]-2-phenyl-1-butanone (20.0 g, 66 mmol) in dry tetrahydrofuran (40 ml) was added and the mixture allowed to warm to room temperature. After 20 hours, the mixture was partitioned between water (200 ml) and ether (200 ml). The ether solution was concentrated and the residual oil dissolved in ethanol (300 ml). Concentrated hydrochloric acid (100 ml) was added, the mixture heated under reflux for 4 hours, then cooled and poured into water (300 ml). The products were extracted with ether (2×150 ml), the combined extracts washed with water (200 ml), dried with sodium sulphate and concentrated to give a brown oil which was dissolvedin ethanol (200 ml). Crystals of mainly 1-[4-(2-chloroethoxy)phenyl]-1-(4-iodophenyl-2-phenyl-1-butene, i.e. the desired trans (E) isomer, of the (2-chloroethoxy)phenyl intermediate, were deposited, recrystallisation of which gave the pure isomer (12.92 g, 40%), m.p. 96°-97° C. Concentration of the original mother liquors gave the cis (Z) isomer (7.03 g, 22%), m.p. 110°-112° C.
Analysis of the crude oil by proton n.m.r. spectroscopy showed that it contained a 1.5:1 mixture of trans (E) and cis (Z) isomers.
A solution of E-1-[4-(2-chloroethoxy)phenyl]-1-(4-iodophenyl)-2-phenyl-1-butene (3.05 g) in 33% diethylamine in ethanol (60 ml) was boiled under reflux for 20 hours. The mixture was concentrated, a procedure made necessary only because of escape of the gaseous dimethylamine under these conditions, further 33% dimethylamine solution (60 ml) was added and reflux was continued for a further 20 hours. The mixture was again concentrated and the residue partitioned between ether (50 ml) and aqueous sodium hydroxide (1M; 50 ml). The ether solution was concentrated and the residue applied to a column of silica gel (Merck 15111, 40 g). Column chromatography was need to remove a small amount of unreacted starting material from the product which could not be removed by recrystallisation. This problem and the concentration step during addition of dimethylamine could have been overcome by carrying out the reaction in a sealed bomb. Elution with 5% methylamine in 1:1 ether-light petroleum (b.p. 40°-60° C.) gave 4-iodotamoxifen, which was further purified by recrystallisation from light petroleum (b.p. 40°-60° C.) (2.60 g, 84% yield), identical to that of Example 1.
The method of Example 3 was used, replacing the dimethylamine addition by a single portion of 1:1 diethylamine-ethanol (v/v) and refluxing for 2 days. 1.069 g of the (2-chloroethoxy)phenyl compound gave 1.03 g (93%) of the title compound, m.p. 58°-59° C. Found: C, 64.10; N, 6.21; N, 2.63; I, 24.12. C28 H32 INO requires C, 64.00; H, 6.14; N, 2.67; I, 24.15%.
The chloroethoxy compound (1.748 g) prepared as in Example 3 and pyrrolidine (10 ml) in ethanol (30 ml) were heated under reflux for 2 hours. The mixture was then concentrated and partitioned between ether (30 ml) and aqueous sodium hydroxide (1M; 30 ml). The ether solution was concentrated and the title compound recrystallised from light petroleum (b.p. 80°-100° C.), yield 1.72 g, (92%), m.p. 108°-109° C. Found: C, 64.28; H, 5.83; N, 2.64; I, 24.06. C28 H30 INO requires C, 64.25; H, 5.78; N, 2.68; I, 24.24%. (Owing to greater reactivity of pyrrolidine than dimethylamine or diethylamine, all the starting material was consumed rapidly and chromatography was not required).
A stirred solution of 1,3-diiodobenzene (5.45 g, 16.5 mmol) in dry tetrahydrofuran (25 ml) at -78° C. under nitrogen was treated with a solution of n-butyl lithium in hexane (1.6M; 10.3 ml, 16.5 mmol). After 5 min, a solution of 1-[4-(2-chloroethoxy)-phenyl]-2-phenyl-1-butene (5.0 g, 16.5 mmol) in dry tetra-hydrofuran (15 ml) was added and the mixture allowed to warm to room temperature. After 20 h, the mixture was poured into water (100 ml) and the products extracted with ether (2×50 ml). The extracts were concentrated under vacuum and the residue dissolved in ethanol (80 ml). Concentrated hydrochloric acid (30 ml) was added and the mixture heated under reflux. After 4 h, the mixture was cooled and partitioned between water (100 ml) and ether (2×60 ml). The ether layers were dried with sodium sulphate, concentrated, and the residue chromatographed on silica gel (Merck 15111, 60 g). Elution with 1:20 l dichloromethane-light petroleum (b.p. 60°-80° C.) gave 1-[4-(chloroethoxy) phenyl]-1-(3-iodophenyl)-2-phenyl-1-butene as a ca. 1.5:1 mixture of E (trans) and Z (cis) isomers (determined by n.m.r. spectroscopy) and as an oil (6.46 g, 80% yield). This mixture (3.63 g) was dissolved in a solution of methylamine (30% w/v) in ethanol, and the resulting solution heated in a sealed vessel at 100° C. for 4 h, then cooled and concentrated to dryness. The residue was partitioned between aqueous sodium hydroxide (100 ml) and ether (100 ml). The ether solution was washed with water (50 ml), dried with sodium sulphate and the residual oil dissolved in cyclohexane (10 ml). Eventually 3-iodotamoxifen crystallised (1.51 g, 41%), m.p. 55°-57° C. NMR: δH (CDCl3, 250 MHz) 0.91 (3H, t, J 7.4 Hz, CH3 CH2), 2.29 (3H, s, NMe2), 2.43 (2H, q, J 7.4 Hz, CH3 CH2), 2.65 (2H, t, J 5.8 Hz, OCH2 CH2 N), 3.93 (2H, t, J 5.8. Hz, OCH2 CH2 N), 6.57 (2H, d, J 8.8 Hz, ArH ortho to side chain), 6.74 (2H, d, J 8.8 Hz, ArH meta to side chain), 7.05-7.26 (7H, m, ArH), 7.58- 7.63 (2H, m, ArH ortho to I).
Relative binding affinities (RBA) of 4-iodo and bromotamoxifen and also of tamoxifen and 4-hydroxytamoxifen for comparison were determined by a rat uterine cytosol test, as follows. Immature rat uterine cytosol was incubated at 18° C. for 30 minutes with 5×10-9 M (3 H)estradiol in the absence and presence of increasing amounts (10-9 -10-5 M) of the test compound or unlabelled estradiol (control). Unbound compounds were then removed with dextran-coated charcoal, and the amounts of estrogen receptor-bound (3 H)estradiol were measured. The relative concentrations of estradiol and test compound required to achieve 50% inhibition of (3 H)estradiol binding are the RBA: RBA=([I50 ](estradiol)/[I50 ](test compound×100.
A whole cell assay was then performed using the MCF-7 human breast cancer cell line obtained from the Michigan Cancer Foundation, Detroit, USA. MCF-7 cells were maintained at 37° C. in monolayer culture in closed T-25 dishes in mininal essential medium (MEM) supplemented with L-glutamine (0.6 mg/ml), gentamycin (40 micrograms/ml). penicillin (100 U/ml) streptomycin (100 micrograms/ml) and 10% inactivated fetal calf serum (inactivated for 1 hour at 56° C.). The MCF-7 cells were incubated at 37° C. for 50 minutes with 10-9 M (3 H)estradiol in the absence or presence of increasing amounts (10-10 -10-5 M) of the test compound or unlabelled estradiol (control). Bound compounds were then extracted with ethanol, and the amounts of estrogen receptor bound (3 H) estradiol were measured. The RBA values were calculated as for the rat uterine cytosol.
The RBA values are shown below in Table 1.
______________________________________ Rat uterine cytosol MCF-7 whole cells______________________________________Tamoxifen 0.5-1.0 0.064-Hydroxytamoxifen 100 2.94-Iodotamoxifen 30 0.054-Bromotamoxifen 3 0.02______________________________________
The higher the values in the rat uterine cytosol test the greater the antiestrogenic effect. In the whole cell test, on the other hand, the estrogen receptors are localised in the cell nucleus and therefore bound to DNA. In the whole cell test, a low value indicating poor binding to cell nucleus ER and consequently low estrogenicity, can be considered favorable.
MCF-7 cells were grown as described in Example 7 and incubated at 37° C. for 24 hours with the test compound at three different concentrations. The test compounds according to the invention used were 3- and 4- iodotamoxifen 4- bromotamoxifen and the analogues of 4-iodotamoxifen in which the dimethylamino group is replaced by diethylamino and pyrrolidino (Examples 4 and 5 respectively). For comparison Z isomers of two of these compounds and tamoxifen itself were tested. Figures in Table 2 below give the percentage cell growth compared with a "blank" sample, and standard deviations obtained from figures for four separate samples of culture. Values greater than 100 indicate a growth stimulating (estrogenic) effect.
TABLE 2______________________________________ MCF-7 Cell Growth,Test Compound (tamoxifen and % of Controlderivatives and analogues Concentration of test compoundthereof) 10-8 M 10-7 M 10-6 M______________________________________4-Iodotamoxifen 115 ± 6 42 ± 6 26 ± 2Z isomer of 4-iodotamoxifen 99 ± 13 126 ± 6 120 ± 3(comparative)3-Iodotamoxifen 100 ± 8 68 ± 2 27 ± 5N,N--diethylamino analogue of 101 ± 7 35 ± 5 23 ± 24-iodotamoxifenPyrrolidino analogue of 84 ± 5 27 ± 3 20 ± 24-iodotamoxifen4-Bromotamoxifen 130 ± 10 101 ± 8 63 ± 8Z isomer of 4-bromotamoxifen 110 ± 3 163 ± 4 174 ± 8(comparative)TAMOXIFEN (comparative) (not tested) 52 ± 1 30 ± 1______________________________________
It will be appreciated from Table 2 that 10-8 M was too low a concentration to differentiate the test compounds adequately and that 10-6 M was more realistic. The results indicate that the 4- iodo pyrrolidino derivative is particularly active, followed by the N,N-diethylamino derivative and the 4-iodo compound itself. The 3-iodo compound was about as active as tamoxifen in these tests, although the large deviation between individual results for this compound makes exact comparison difficult. The 4-bromo compound appeared less active than tamoxifen in these tests, in contrast to those of Example 7.
Following the procedure of Example 3 of U.S. Pat. No. 4,536,516 (ICI), 50 parts of 4l -iodotamoxifen, 42 parts of maize starch and 7 parts of alginic acid are intimately mixed and granulated using 10% maize starch paste as the granulating agent. The granules are dried at a temperature not exceeding 50° C., and then mixed with 1 part of magnesium stearate and compressed into tablets each weighing 50 mg. There are thus obtained tablets suitable for oral administration for therapeutic purposes.
Preparation of 4-iodotamoxifen from 4-bromotamoxifen
This Example shows that 4-bromotamoxifen is readily convertible into 4-iodotamoxifen. The Example was carried out using ordinary ("cold", non-radioisotopic) molecular iodine, for reasons of laboratory safety but could obviously be repeated substituting a radioisotopic iodine for ordinary iodine.
To a stirred solution of E-1-[4-[2-dimethylamino)ethoxy]-1-(4-bromophenyl)-2-phenyl-1-butene (146.5 mg, 0.325 mmol) in tetrahydrofuran (1 ml) cooled to ca.-75° C. under an atmosphere of nitrogen was added a solution of tert-butyllithium in pentane (1.8M; 0.27 ml, 0.488 mmol). After 5 min, a solution of iodine (101.5 mg, 0.40 mmol) in tetrahydrofuran (1 ml) was added and the mixture allowed to warm to room temperature, then diluted with water (5 ml) and extracted with ether (2×5 ml). The ether solution was dried with sodium sulphate and concentrated. The residual oil was virtually entirely 4-iodotamoxifen by NMR. The product was recrystallized from light petroleum, b.p. 60°-80° C. Yield 108.6 mg, 67%, m.p. 110° C. (previously recorded m.p. 112°-114° C.).
Note that half of the iodine is lost as iodide by the reaction Ar+I2 +ArI+I- (where Ar represents the residue of the tamoxifen molecule). In a radiolabelled synthesis it would be advisable to add first a portion less than an equivalent and I2 of radioisotopic iodine, then "cold" iodine to bring the reaction to completion.
8 mg of "cold" 4-iodotamoxifen were dissolved in 1:1 ethanol-ethyl acetate. To this solution was added 25 μl of a solution prepared by dissolution of 12 mg copper (II) sulphate in 500 μl methanol, and also 5 μl of a solution of sodium iodide-125 (ca.100 μl Ci) in dilute sodium hydroxide. This mixture was heated for 1 h at 106°-107° C. in a 2 ml sealed vessel ("Reacti-vial"). Thin layer chromatography on silica gel (eluant 1:1 v/v ethanol-ethyl acetate or 4:4:1 v/v/v petroleum ether-diethyl ether-triethylamine) indicated more than 99% exchange labelling.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3288806 *||Mar 23, 1964||Nov 29, 1966||Parke Davis & Co||Alpha-(aminoethoxyphenyl)-alpha-alkylstilbenes|
|1||*||A. B. Foster et al., J. Med. Chem., 28, 1491 1497 (1985).|
|2||A. B. Foster et al., J. Med. Chem., 28, 1491-1497 (1985).|
|3||*||D. H. Hunter et al., Appl. Radiat. Isot., 37, 889 891 (1986).|
|4||D. H. Hunter et al., Appl. Radiat. Isot., 37, 889-891 (1986).|
|5||*||D. H. Hunter et al., Can. J. Chem., 61, 421 426 (1983).|
|6||D. H. Hunter et al., Can. J. Chem., 61, 421-426 (1983).|
|7||*||D. W. Robertson et al., J. Med. Chem., 25, 167 171 (1982).|
|8||D. W. Robertson et al., J. Med. Chem., 25, 167-171 (1982).|
|9||*||G. L. Tonnensen et al., Int. J. Radiat. Isot., 32, 171 173 (1981).|
|10||G. L. Tonnensen et al., Int. J. Radiat. Isot., 32, 171-173 (1981).|
|11||*||G. Leclercq et al., J. Steroid. Biochem., 19, 75 85 (1983).|
|12||G. Leclercq et al., J. Steroid. Biochem., 19, 75-85 (1983).|
|13||*||K. E. Allen et al., British Journal of Pharmacology, 71, 83 91 (1980).|
|14||K. E. Allen et al., British Journal of Pharmacology, 71, 83-91 (1980).|
|15||*||L. Maddedu et al., Anticancer Research, 6, 11 16 (1986).|
|16||L. Maddedu et al., Anticancer Research, 6, 11-16 (1986).|
|17||Lieberman et al., "Inhibition of Estradiol-Stumulated Prolactin Synthesis", J. Biol. Chem., 1983, 258(8), 4734-40, [Chemical Abstracts, vol. 99, 1983, p. 77].|
|18||*||Lieberman et al., Inhibition of Estradiol Stumulated Prolactin Synthesis , J. Biol. Chem., 1983, 258(8), 4734 40, Chemical Abstracts, vol. 99, 1983, p. 77 .|
|19||*||M. M. King et al., Journal of National Cancer Institute, 74, 447 451 (1985).|
|20||M. M. King et al., Journal of National Cancer Institute, 74, 447-451 (1985).|
|21||Sham et al., "Fluorotamoxifen", J. Med. Chem., 1985, 28(10), 1504-11, [Chemical Abstracts, vol. 103, 1985, p. 341].|
|22||*||Sham et al., Fluorotamoxifen , J. Med. Chem., 1985, 28(10), 1504 11, Chemical Abstracts, vol. 103, 1985, p. 341 .|
|23||*||W. D. Bloomer et al., Int. J. Radiat. Biol., 38, 197 202 (1980).|
|24||W. D. Bloomer et al., Int. J. Radiat. Biol., 38, 197-202 (1980).|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US5192525 *||Jun 28, 1991||Mar 9, 1993||Board Of Regents, The University Of Texas System||High affinity tamoxifen derivatives and uses thereof|
|US5219548 *||Oct 1, 1990||Jun 15, 1993||Board Of Regents, The University Of Texas System||High affinity halogenated-tamoxifen derivatives and uses thereof|
|US5410080 *||Feb 10, 1994||Apr 25, 1995||Merrell Dow Pharmaceuticals Inc.||Non-metabolizable clomiphene analogs for treatment of tamoxifen-resistant tumors|
|US5472985 *||Sep 2, 1994||Dec 5, 1995||Neorx Corporation||Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells|
|US5545569 *||May 25, 1995||Aug 13, 1996||Neorx Corporation||Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells|
|US5595722 *||Jun 7, 1995||Jan 21, 1997||Neorx Corporation||Method for identifying an agent which increases TGF-beta levels|
|US5599844 *||Sep 15, 1995||Feb 4, 1997||Neorx Corporation||Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells|
|US5681863 *||Dec 5, 1994||Oct 28, 1997||Merrell Pharmaceuticals Inc.||Non-metabolizable clomiphene analogs for treatment of tamoxifen-resistant tumors|
|US5693863 *||Jan 3, 1994||Dec 2, 1997||Klinge Pharma Gmbh||Method for the production of E-1- 4'- (2- Dimethylaminoethoxy) - Phenyl!-1-(3-Hydroxyphenyl) -2-Phenyl-1-Butene|
|US5733925 *||Oct 28, 1996||Mar 31, 1998||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US5770609 *||Jun 7, 1995||Jun 23, 1998||Neorx Corporation||Prevention and treatment of cardiovascular pathologies|
|US5773479 *||Nov 21, 1995||Jun 30, 1998||Neorx Corporation||Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells|
|US5811447 *||May 25, 1995||Sep 22, 1998||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US5847007 *||May 12, 1994||Dec 8, 1998||Neorx Corporation||Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells|
|US5945456 *||Nov 6, 1997||Aug 31, 1999||Neorx Corporation||Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells|
|US5981568 *||Mar 31, 1997||Nov 9, 1999||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US6074625 *||Feb 28, 1997||Jun 13, 2000||Neutron Therapies Inc.||Boron-containing hormone analogs and methods of their use in imaging or killing cells having hormone receptors|
|US6074659 *||Jul 10, 1998||Jun 13, 2000||Noerx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US6096874 *||Jun 7, 1995||Aug 1, 2000||Board Of Regents, The University Of Texas System||High affinity tamoxifen derivatives|
|US6117911 *||Apr 9, 1998||Sep 12, 2000||Neorx Corporation||Compounds and therapies for the prevention of vascular and non-vascular pathologies|
|US6166090 *||Nov 6, 1997||Dec 26, 2000||Neorx Corporation||Prevention and treatment of pathologies associated with abnormally proliferative smooth muscle cells|
|US6197789||Jun 7, 1996||Mar 6, 2001||Neorx Corporation||Prevention and treatment of cardiovascular pathologies with tamoxifen analogues|
|US6251920||May 21, 1998||Jun 26, 2001||Neorx Corporation||Prevention and treatment of cardiovascular pathologies|
|US6262079||May 6, 1999||Jul 17, 2001||Neorx Corporation||Prevention and treatment of cardiovascular pathologies|
|US6268390||Dec 22, 1999||Jul 31, 2001||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US6306421||Mar 31, 1997||Oct 23, 2001||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US6358989||Jul 26, 1999||Mar 19, 2002||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US6395494||Jun 7, 1995||May 28, 2002||Neorx Corporation||Method to determine TGF-β|
|US6410587||May 5, 2000||Jun 25, 2002||Neorx Corporation||Compounds and therapies for the prevention of vascular and non-vascular pathologies|
|US6491938||Jun 29, 2001||Dec 10, 2002||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US6569441||Nov 27, 2001||May 27, 2003||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US6663881||Dec 18, 2001||Dec 16, 2003||Neorx Corporation||Therapeutic inhibitor of vascular smooth muscle cells|
|US6720350||Dec 27, 2002||Apr 13, 2004||Scimed Life Systems, Inc.||Therapeutic inhibitor of vascular smooth muscle cells|
|US6875775||Apr 8, 2003||Apr 5, 2005||Hormos Medical Oy Ltd||Triphenylalkene derivatives and their use as selective estrogen receptor modulators|
|US7084171||Apr 19, 2004||Aug 1, 2006||Neorx Corporation||Compounds and therapies for the prevention of vascular and non-vascular pathologies|
|US7094550||Mar 26, 2002||Aug 22, 2006||Neorx Corporation||Method to determine TGF-beta|
|US7446121||Nov 18, 2005||Nov 4, 2008||Pfizer Inc.||Pyrazole-based HMG CoA reductase inhibitors|
|US7449453||Jul 13, 2006||Nov 11, 2008||Karykion Inc.||Compositions of ezetimibe and methods for the treatment of cholesterol-associated benign and malignant tumors|
|US7511070||Nov 9, 2005||Mar 31, 2009||Poniard Pharmaceuticals, Inc.||Compounds and therapies for the prevention of vascular and non-vascular pathologies|
|US7625410||Jan 23, 2006||Dec 1, 2009||Boston Scientific Scimed, Inc.||Stent device and method|
|US7825107||May 22, 2007||Nov 2, 2010||Hormos Medical Ltd.||Method of treating men suffering from chronic nonbacterial prostatitis with SERM compounds or aromatase inhibitors|
|US8067022||Jul 20, 2001||Nov 29, 2011||Boston Scientific Scimed, Inc.||Therapeutic inhibitor of vascular smooth muscle cells|
|US8097642||Feb 27, 2007||Jan 17, 2012||Boston Scientific Scimed, Inc.||Therapeutic inhibitor of vascular smooth muscle cells|
|US8158670||Jan 4, 2007||Apr 17, 2012||Boston Scientific Scimed, Inc.||Therapeutic inhibitor of vascular smooth muscle cells|
|US8962693||Aug 19, 2013||Feb 24, 2015||Hormos Medical Ltd.||Method for the treatment or prevention of lower urinary tract symptoms|
|US20050020667 *||Apr 19, 2004||Jan 27, 2005||Grainger David J.||Compounds and therapies for the prevention of vascular and non-vascular pathologies|
|US20050070512 *||Sep 16, 2004||Mar 31, 2005||Pfizer Inc||Pharmaceutical composition and methods comprising combinations of 2-alkylidene-19-nor-vitamin D derivatives and an estrogen agonist/antagonist|
|US20050203086 *||Mar 4, 2004||Sep 15, 2005||Pfizer Inc.||Methods of treatment using an EP2 selective receptor agonist|
|US20060029986 *||Sep 20, 2005||Feb 9, 2006||Grainger David J||Prevention and treatment of cardiovascular pathologies|
|EP1932543A2||Dec 23, 1996||Jun 18, 2008||Pfizer, Inc.||Combination therapy for osteoporosis consisting of an estrogen agonist/antagonist and a growth hormone secretagogue|
|WO1996040616A1 *||Jun 7, 1996||Dec 19, 1996||Univ Texas||High affinity tamoxifen derivatives and uses thereof|
|WO1998009619A1 *||Sep 3, 1997||Mar 12, 1998||Beesley Jacqueline & Hf||Novel methods|
|WO1999000018A1 *||Jun 26, 1998||Jan 7, 1999||Macdonald Brian R||Methods of treating symptoms of impaired memory, concentration and cognition in postmenopausal women|
|WO1999000019A1 *||Jun 26, 1998||Jan 7, 1999||Macdonald Brian R||Methods of treating the symptoms of atrophic vaginitis and altered sexual behavior in postmenopausal women|
|WO1999002509A1 *||Jul 7, 1998||Jan 21, 1999||Nigel Hussain||Process for preparing tri-aryl-alkylalkenes|
|WO2007143607A2||Jun 4, 2007||Dec 13, 2007||Pear Tree Women S Health Care||Method of treating atrophic vaginitis|
|WO2009019504A1||Aug 1, 2008||Feb 12, 2009||Summit Corp Plc||Drug combinations for the treatment of duchenne muscular dystrophy|
|WO2009019505A2||Aug 1, 2008||Feb 12, 2009||Summit Corp Plc||Drug combinations for the treatment of duchenne muscular dystrophy|
|WO2013130832A1||Feb 28, 2013||Sep 6, 2013||Repros Therapeutics Inc.||Combination therapy for treating androgen deficiency|
|U.S. Classification||424/1.85, 514/651, 514/648, 514/239.2, 424/1.45, 544/174, 548/575, 514/317, 564/324, 514/428, 546/236|
|International Classification||A61K31/138, C07D295/08, C07D295/092, C07C213/00, A61K51/00, A61P35/00, C07C67/00, A61K31/395, A61K31/135, C07C217/18, A61K51/04|
|Cooperative Classification||A61K51/0406, C07D295/088, A61K51/0446|
|European Classification||A61K51/04G60F, A61K51/04D4, C07D295/088|
|Apr 7, 1989||AS||Assignment|
Owner name: NATIONAL RESEARCH DEVELOPMENT CORPORATION, ENGLAND
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:MCCAGUE, RAYMOND;REEL/FRAME:005044/0139
Effective date: 19870824
|Aug 11, 1992||AS||Assignment|
Owner name: BRITISH TECHNOLOGY GROUP LIMITED, ENGLAND
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:NATIONAL RESEARCH DEVELOPMENT CORPORATION;REEL/FRAME:006243/0136
Effective date: 19920709
|Nov 13, 1992||FPAY||Fee payment|
Year of fee payment: 4
|Dec 9, 1996||FPAY||Fee payment|
Year of fee payment: 8
|Jan 2, 2001||REMI||Maintenance fee reminder mailed|
|Jan 17, 2001||SULP||Surcharge for late payment|
Year of fee payment: 11
|Jan 17, 2001||FPAY||Fee payment|
Year of fee payment: 12